| 111. |
- Ma, Zaifei, et al.
(författare)
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Structure-Property Relationships of Oligothiophene-Isoindigo Polymers for Efficient Bulk-Heterojunction Solar Cells
- 2014
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Ingår i: energy and environmental science. - : Royal Society of Chemistry. - 1754-5692. ; 17:1, s. 361-369
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Tidskriftsartikel (refereegranskat)abstract
- A series of alternating oligothiophene (nT)-isoindigo (I) copolymers (PnTI) were synthesized to investigate the influence of the oligothiophene block length on the photovoltaic (PV) properties of PnTI:PCBM bulk-heterojunction blends. Our study indicates that the number of thiophene rings (n) in the repeating unit alters both, polymer crystallinity and polymer-fullerene interfacial energetics, which results in a decreasing open-circuit voltage (Voc) of the solar cells with increasing n. The short-circuit current density (Jsc) of P1TI:PCBM devices is limited by the absence of a significant driving force for electron transfer. Instead, blends based on P5TI and P6TI feature large polymer domains, which limit charge generation and thus Jsc. The best PV performance with a power conversion efficiency of up to 6.9% was achieved with devices based on P3TI, where a combination of favorable morphology and optimal interface energy level offset ensures efficient exciton separation and charge generation. The structure-property relationship demonstrated in this work is a valuable guideline for the design of high performance polymers with small energy losses during the charge generation process, allowing for the fabrication of efficient solar cells that combine a minimal loss in Voc with a high Jsc.
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| 112. |
- Ma, Zaifei, 1986-
(författare)
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Studies of Morphology and Charge-Transfer in Bulk-Heterojunction Polymer Solar Cells
- 2013
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The work presented in this thesis focuses on the two critical issues of bulk-heterojunction polymer solar cells: morphology of active layers and energy loss during charge transfer process at electron donor/acceptor interfaces. Both issues determine the performance of polymer solar cells through governing exciton dissociation, charge carrier recombination and free charge carrier transport.The morphology of active layers (spatial percolation of the donor and acceptor) is crucial for the performance of polymer solar cells due to the limited diffusion length of excitons in organic semiconductors (5-20 nm). Meanwhile, the trade-off between charge generation and transport also needs to be considered. On the one hand, a finely mixed morphology with a large donor/acceptor interface area is preferred for charge generation because efficient exciton dissociation only occurs at the interface, but on the other hand, proper phase separation is needed to reduce charge carrier recombination and facilitate free charge carrier transport to the electrodes. In this thesis, morphologies of the active layers based on different polymeric donors and fullerene acceptors are correlated to the performance of solar cells with various microscopic and spectroscopic techniques including atomic force microscope, transmission electron microscope, grazing incidence x-ray diffraction, photoluminescence, electroluminescence and Fourier transform photocurrent spectroscopy. Furthermore, methods to manipulate the morphologies of solution processed active layers to achieve high performance solar cells are also presented. Processing solvents, chemical structures of the donor and the acceptor materials, and substrate surface properties are found critically important in determining the nanoscale phase separation and performance of polymer solar cells.Optimizing morphology of active layers alone does not guarantee high performance devices. In addition to spatial percolation, energy arrangements of donors and acceptors are also essential due to contrary requests of the photocurrent and the photovoltage: Efficient exciton dissociation or charge transfer at donor/acceptor interfaces requires large enough energetic driving force, which is also known as energy loss for charge transfer. However, the energy loss due to charge transfer will unavoidably reduce the photovoltage. In this thesis the balance between the photocurrent and the photovoltage in polymer solar cells due to charge transfer at donor/acceptor interfaces is investigated for different active material systems. The driving force tuned by synthesizing series of polymers is determined by directly measuring the optical band gap via UV-Vis spectroscopy and probing the charge transfer recombination via electroluminescence measurements. Influences of driving force on the photocurrent and the photovoltage are characterized via field dependent photoluminescence and internal quantum efficiency measurements. The results correlated well with the performance of the solar cells.
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| 113. |
- Ma, Zaifei, et al.
(författare)
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Synthesis and characterization of benzodithiophene-isoindigo polymers for solar cells
- 2012
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Ingår i: Journal of Materials Chemistry. - : Royal Society of Chemistry (RSC). - 1364-5501 .- 0959-9428. ; 22:5, s. 2306-2314
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Tidskriftsartikel (refereegranskat)abstract
- Three new alternating polymers with the electron-deficient isoindigo group as the acceptor unit and benzo[1,2-b:4,5-b'] dithiophene (BDT) or BDT flanked by thiophenes (or octylthiophenes) as the donor unit were designed and synthesized. All the polymers have good thermal stability, solubility and broad absorption spectra. Their photophysical, electrochemical and photovoltaic (PV) properties were investigated. To understand their different PV performance in the resulting polymer solar cells (PSCs), the morphology of their blends with fullerene derivatives was investigated by atomic force microscopy, and the molecular geometries as well as the molecular frontier orbitals were simulated by density functional theory calculations (Gaussian 09). The polymer PBDT-TIT, with BDT flanked by thiophenes as the donor unit and isoindigo as the acceptor unit, exhibits quite planar backbones and its blend with fullerene derivatives shows optimal morphology. As a result, the PSCs based on PBDT-TIT with a conventional device configuration of ITO/PEDOT: PSS/PBDT-TIT: PC(61)BM/LiF/Al showed a power conversion efficiency of 4.22%, with a short-circuit current density of 7.87 mA cm(-2), an open-circuit voltage of 0.79 V and a fill factor of 0.68 under the AM 1.5G illumination with an intensity of 100 mW cm(-2) from a solar simulator.
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| 114. |
- Mammo, W., et al.
(författare)
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New low band gap alternating polyfluorene copolymer-based photovoltaic cells
- 2007
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248 .- 1879-3398. ; 91:11, s. 1010-1018
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Tidskriftsartikel (refereegranskat)abstract
- New low band gap alternating polyfluorene copolymers were synthesized for use in plastic solar cells and their optical, electrochemical, and photovoltaic characteristics were determined. These polymers incorporated fluorene units alternating with groups including electron-withdrawing (A) and electron-donating (D) groups in donor-acceptor-donor (DAD) sequence to achieve the lowering of band gaps. The HOMO-LUMO values were estimated from electrochemical studies. By varying the donor and acceptor strength and position of the solubilizing substituents, similar HOMO values were obtained. These values were also found to correlate well with the open circuit voltage (VOC) values determined from photovoltaic data of the polymers blended with the acceptor PCBM. Despite similar HOMO values, the absorption spectra of the polymers differ significantly. This prompted the preparation of photovoltaic devices consisting of blends of two polymers with complementary absorptions in combination with PCBM to harvest more photons in the polymer solar cells. © 2007 Elsevier B.V. All rights reserved.
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| 115. |
- Mammo, Wendimagegn, 1954, et al.
(författare)
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New low band gap alternating polyfluorene copolymer-based photovoltaic cells
- 2007
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Ingår i: Sol. Energy Mater. Sol. Cells FIELD Full Journal Title:Solar Energy Materials & Solar Cells. ; 91:11, s. 1010-1018
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Tidskriftsartikel (refereegranskat)abstract
- New low band gap alternating polyfluorene copolymers were synthesized for use in plastic solar cells and their optical, electrochem., and photovoltaic characteristics were detd. These polymers incorporated fluorene units alternating with groups including electron-withdrawing (A) and electron-donating (D) groups in donor-acceptor-donor (DAD) sequence to achieve the lowering of band gaps. The HOMO-LUMO values were estd. from electrochem. studies. By varying the donor and acceptor strength and position of the solubilizing substituents, similar HOMO values were obtained. These values were also found to correlate well with the open circuit voltage (VOC) values detd. from photovoltaic data of the polymers blended with the acceptor PCBM. Despite similar HOMO values, the absorption spectra of the polymers differ significantly. This prompted the prepn. of photovoltaic devices consisting of blends of two polymers with complementary absorptions in combination with PCBM to harvest more photons in the polymer solar cells. [on SciFinder (R)]
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| 116. |
- Martin, N. M., et al.
(författare)
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CO Adsorption on Clean and Oxidized Pd(111)
- 2014
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Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 118:2, s. 1118-1128
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption of CO on clean and oxidized Pd(111) surfaces has been investigated using a combination of high-resolution core level spectroscopy (HRCLS), reflection absorption infrared spectroscopy (RAIRS), and density functional theory (DFT) calculations. The HRCLS and RAIRS measurements reveal that CO adsorbs on Pd(111), Pd(5)O4 and PdO(101) at 100 +/- 10 K and that the CO coverage decreases with increasing oxidation state of Pd for the same CO exposures of 10 Langmuirs. Based on the DFT calculations, the CO layer on clean Pd(111) was found to include molecular adsorption in both hollow and bridge sites, whereas CO occupies a combination of bridge and atop sites on the Pd5O4 and PdO(101) surfaces.
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| 117. |
- Murthy, D H K, et al.
(författare)
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Origin of Reduced Bimolecular Recombination in Blends of Conjugated Polymers and Fullerenes
- 2013
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Ingår i: Advanced Functional Materials. - : Wiley-VCH Verlag. - 1616-301X .- 1616-3028. ; 23:34, s. 4262-4268
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Tidskriftsartikel (refereegranskat)abstract
- Bimolecular charge carrier recombination in blends of a conjugated copolymer based on a thiophene and quinoxaline (TQ1) with a fullerene derivative ((6,6)-phenyl-C-71-butyric acidmethyl ester, PC71BM) is studied by two complementary techniques. TRMC (time-resolved microwave conductance) monitors the conductance of photogenerated mobile charge carriers locally on a timescale of nanoseconds, while using photo-CELIV (charge extraction by linearly increasing voltage) charge carrier dynamics are monitored on a macroscopic scale and over tens of microseconds. Despite these significant differences in the length and time scales, both techniques show a reduced Langevin recombination with a prefactor close to 0.05. For TQ1:PC71BM blends, the value is independent of temperature. On comparing TRMC data with electroluminescence measurements it is concluded that the encounter complex and the charge transfer state have very similar energetic properties. The value for annealed poly(3-hexylthiophene) (P3HT):(6,6)-phenyl-C-61-butyric acid methyl ester (PC61BM) is approximately 10(-4), while for blend systems containing an amorphous polymer values are close to 1. These large differences can be related to the extent of charge delocalization of opposite charges in an encounter complex. Insight is provided into factors governing the bimolecular recombination process, which forms a major loss mechanism limiting the efficiency of polymer solar cells.
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| 118. |
- Nemec, Hynek, et al.
(författare)
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Charge carrier dynamics in alternating polyfluorene copolymer : Fullerene blends probed by terahertz spectroscopy
- 2008
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 112:16, s. 6558-6563
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Tidskriftsartikel (refereegranskat)abstract
- Time-resolved terahertz spectroscopy is used for investigation of photoinduced charge carrier dynamics in blends of a polyfluorene copolymer (poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4',7'-di-2-thienyl- 2',1',3-benzo-thiadiazole)]) and an electron acceptor ([6,6]-phenyl-C61-butyric acid methyl ester). The transient far-infrared response appears instantaneously after photoexcitation. We show that the transient conductivity spectrum is dominated by two major contributions: response of separated charge carriers and response of coupled polaron pairs. © 2008 American Chemical Society.
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| 119. |
- Nemec, Hynek, et al.
(författare)
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Sub-Picosecond Time-Dependent Mobility in Low-Band-Gap Polyphenylene:Fullerene Blend Probed by Terahertz Spectroscopy
- 2008
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Ingår i: Conference on Lasers and Electro-Optics, 2008 and 2008 Conference on Quantum Electronics and Laser Science. CLEO/QELS 2008. - : IEEE. - 1092-8081. - 9781557528599 ; , s. 3108-3109
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Konferensbidrag (refereegranskat)abstract
- Time-resolved terahertz spectroscopy is used to investigate photoinduced dynamics of charge carriers in a polymer heterojunction. We directly observe instantaneous generation of highly mobile charge carriers followed by a rapid drop in their mobility. (C) 2008 Optical Society of America
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| 120. |
- Nemec, Hynek, et al.
(författare)
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Ultrafast conductivity in a low-band-gap polyphenylene and fullerene blend studied by terahertz spectroscopy
- 2009
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Ingår i: Physical Review B - Condensed Matter and Materials Physics. - 2469-9950 .- 2469-9969 .- 1098-0121. ; 79:24, s. 245326 (art no)-
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Tidskriftsartikel (refereegranskat)abstract
- Time-resolved terahertz spectroscopy and Monte Carlo simulations of charge-carrier motion are used to investigate photoinduced transient conductivity in a blend of a low-band-gap polyphenylene copolymer and fullerene derivative. The optical excitation pulse generates free holes delocalized on polymer chains. We show that these holes exhibit a very high initial mobility as their initial excess energy facilitates their transport over defects (potential barriers) on polymer chains. The conductivity then drops down rapidly within 1 ps, and we demonstrate that this decrease occurs essentially by two mechanisms. First, the carriers loose their excess energy and they thus become progressively localized between the on-chain potential barriers-this results in a mobility decay with a rate of (180 fs)(-1). Second, carriers are trapped at defects (potential wells) with a capture rate of (860 fs)(-1). At longer time scales, populations of mobile and trapped holes reach a quasiequilibrium state and further conductivity decrease becomes very slow.
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